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A form for completing the data required by various international classification bodies to express an opinion on the activities and performance of Assiut University.

A form for completing the data required by various international classification bodies to express an opinion on the activities and performance of Assiut University.

السادة الأفاضل  اعضاء هيئة التدريس في الجامعات الحكومية و الاهلية و الخاصة داخل مصر و خارجها 


 كل عام وحضراتكم بخير
   إيمانا من جامعة أسيوط بأهمية التواصل مع اعضاء هيئة التدريس من الجامعات المختلفة وحرصا من الجامعة على التقدم في التصنيفات الأكاديمية المختلفة
 لذا الرجاء من السادة الزملاء اعضاء هيئة التدريس داخل مصر وخارجها     الدخول على الرابط التالي لاستكمال البيانات المطلوبة لتكون مرجعا لهيئات التصنيفات الدولية المختلفة لإبداء الرأي عن أنشطة وأداء جامعة أسيوط.

https://forms.gle/zt7DV8ZRHbLTHp4B9
   
   مكتب التصنيف الأكاديمي الدولي


Dear National and international professors 
We wish you a Happy New Year.   
Our university believes in the importance of communicating with you and advancing in the various academic ranking.
So, dear professors inside Egypt or outside who do not work within our university, please check the following link to complete the required data to be a reference for the various international university ranking bodies to give an opinion about the performance and activities of our university.
 
https://forms.gle/zt7DV8ZRHbLTHp4B9

Assiut university international ranking offcice

Announcement regarding the opening of applications for the UNESCO King Hamad bin Isa Al Khalifa Prize for the Use of Information and Communication Technology in the Field of Education for the year 2023.

Announcement regarding the opening of applications for the UNESCO King Hamad bin Isa Al Khalifa Prize for the Use of Information and Communication Technology in the Field of Education for the year 2023.

Announcement regarding the opening of applications for the UNESCO King Hamad bin Isa Al Khalifa Prize for the Use of Information and Communication Technology in the Field of Education for the year 2023.

High Versus Low Dose of Magnesium Sulfate as Initial Tocolytic Agent for Preterm Labour in Symptomatic Placenta Previa

Research Abstract

Objective

To assess the efficacy and safety of alternative magnesium sulfate regimens used as single tocolytic therapy for preventing preterm labor in patients with symptomatic placenta previa and subsequent changes in cervical length.

Methods

The study was a randomized clinical trial conducted from December 2020 to August 2022 at Assiut Women's Health Hospital, Egypt, including pregnant women from 28 to 37 weeks of gestation with a singleton fetus in PTL and symptomatic placenta previa. The eligible women were randomized to either (group 1 or 2). The primary outcome was evaluating the efficacy of two different regimens of magnesium sulfate in postponing delivery in patients with P.P. in PTL for 48 hours and changes in cervical length.

Results

Clinical and pregnancy prolongation data showed no significant difference between the two therapy regimens. The high-dose group had a considerably longer cervical length (cm) at 48 hours (p<0.001). The low-dose group had a lower 4-hour magnesium serum level (3.98±0.60 vs. 4.80±0.91; p<0.001). Furthermore, when comparing subgroups based on obesity, our analysis revealed a significant increase in non-obese women delivering after 48 hours in high and low groups. Cervical length after 48 hours (cm) was also increased in the non-obese high-dose group (p<0.030). Non-obese pregnancies treated with high-maintenance tocolysis achieve a therapeutic level of magnesium than obese patients(36.1% vs.6.9%, p=0.007).

Conclusions

A high magnesium sulfate regimen in symptomatic preterm P,P in non-obese women may be related to potential clinical prolongation of pregnancy, an …

Research Authors
M Ibrahim, E Elsenosy, D Mostafa, M Seddik, M Ali
Research Date
Research Journal
Evidence Based Women's Health Journal 13 (2), 183-191
Research Pages
183-191
Research Publisher
Evidence Based Women’s Health Society
Research Vol
Volume 13, Issue 2
Research Website
https://scholar.google.com.eg/scholar?oi=bibs&cluster=5873946907827230377&btnI=1&hl=en
Research Year
2023

Systemic Analgesia versus Continuous Erector Spinae Plane Block (ESPB) Infusion During Paediatric Nephrectomy: A Randomized, Controlled Trial

Research Authors
S Adlan, A Abd El-Rahman, SAB Mohamed, AM Thabet, EM Hamada, ...
Research Date
Research Journal
Local and Regional Anesthesia, 59-69

The effect of dexmedetomidine versus propofol in traumatic brain injury evaluation of some hemodynamic and intracranial pressure changes

Research Authors
M Khallaf, AM Thabet, M Ali, E Sharkawy, S Abdel-rehim
Research Date
Research Journal
Egyptian Journal of Neurosurgery 34 (1), 1-10

Trichloroacetic Acid With Microneedling Versus Trichloroacetic Acid Alone for Treating Melasma

Research Abstract

Abstract

BACKGROUND 

Melasma is a common acquired disorder of hyperpigmentation which is difficult to treat.

OBJECTIVE 

We aim to evaluate the efficacy and safety of combined microneedling with trichloroacetic acid in the treatment of melasma.

PATIENTS AND METHODS 

Forty women with facial melasma were included and randomly classified into 2 groups. Group A included 20 patients treated with bimonthly session of trichloroacetic acid 25% peeling (8 sessions) combined with a monthly session of microneedling (4 sessions). Group B included the other 20 patients that were treated by bimonthly trichloroacetic acid 25% peeling session (8 sessions) alone.

RESULTS 

After 1 and 3 months of treatment, the mean melasma area and severity index, modified melasma area and severity index, and melasma severity index scores showed significant improvement in each group (p < .05 for each). At 1 and 3 months, the mean percentages of change of all scores were significantly higher in group A than group B (p < .05).

CONCLUSION 

Combined trichloroacetic acid peel with microneedling is effective and a safe option for treating melasma.

Research Authors
Eman R Hofny, Amira A Abdel-Motaleb, Safaa Ahmed Hamed, Howida Omar Twisy
Research Date
Research Department
Research Pages
66-71
Research Publisher
LWW
Research Vol
49
Research Year
2023

Which is more effective in atrophic acne scars treatment microneedling alone or platelet rich plasma alone or combined both therapeutic modalities?

Research Abstract

Acne scarring usually causes cosmetic and psychological problems. Our aim of the study was to compare the efficacy of microneedling alone, intradermal injection of platelet rich plasma (PRP) alone and combined microneedling with PRP in the treatment of atrophic post‐acne scars. Thirty adult patients with facial post‐acne scars were randomly recruited and divided into two groups: A and B. Group A: included 15 patients; the left sides of their faces were treated with microneedling by dermapen followed by PRP while on the right side of the faces microneedling alone was performed. Group B: included 15 patients; the left sides of their faces were treated with microneedling by dermapen followed by PRP while the right sides of the faces were treated with intradermal injection of PRP. For both groups, the treatment session was repeated every 3 weeks until clearance of the atrophic acne scars or for four sessions …

Research Authors
Sahar A Ismail, Nanis AH Khella, Doaa AE Abou‐Taleb
Research Date
Research Department
Research Journal
Dermatologic Therapy
Research Pages
e15925
Research Publisher
John Wiley & Sons, Inc.
Research Rank
َQ1
Research Vol
Volume35, Issue12
Research Website
https://onlinelibrary.wiley.com/doi/full/10.1111/dth.15925
Research Year
2022

Significant Interrelations among Serum Annexin A1, Soluble Receptor for Advanced Glycation End Products (sRAGE) and rs2070600 in Chronic Obstructive Pulmonary Disease

Research Abstract

Chronic obstructive pulmonary disease (COPD) is a major cause of death and morbidity; it may be accompanied by oxidative stress and inflammation with or without underlying genetic etiology. Finding circulating biomarkers for COPD that can help early diagnosis and predict exacerbation and association with respiratory functions has been challenging. There were 40 healthy participants and 60 COPD patients in this research. The rs2070600 gene variant was examined by PCR-RFLP. Circulating sRAGE and annexin A1 levels were determined by ELISA. GSH and MDA were determined by

Research Authors
Amira A Kamel, Maiada K Hashem, Ebtsam S AbdulKareem, Amal H Ali, Ekram Abdel-Rahman Mahmoud, Alaa S Abd-Elkader, Hebatallah Abdellatif, Alzahra Abdelbadea, Nessren M Abdel-Rady, Mona Gamal E Al Anany, Marwa A Dahpy
Research Date
Research Department
Research Journal
Biology
Research Pages
1707
Research Publisher
MDPI
Research Vol
12
Research Year
2022

Fractional carbon dioxide laser alone and as an assisted drug delivery for treatment of alopecia areata: a clinical, dermoscopic and immunohistochemical study

Research Abstract

Alopecia areata (AA) is a common cause of hair loss with no available universally successful treatment. Thus, new innovative treatments are urgently needed. This research aimed to evaluate the effectiveness of fractional carbon dioxide laser (FCL) alone or combined with triamcinolone acetonide (TA) solution, platelet-rich plasma (PRP), or vitamin D3 solution in treating AA. Sixty-four AA patients with 185 lesions were recruited and divided into four treatment groups. All patients received FCL either alone (group A, n = 19) or followed by topical TA (group B, n = 16) or PRP (group C, n = 15), or vitamin D3 solution (group D, n = 14). The response was assessed using Alopecia Areata Severity Index (AASI), MacDonald Hull and Norris grading, and trichoscopy. Histopathological features and immunohistochemical decorin expression were studied. All groups showed significant improvement in AASI compared to the baseline, with insignificant differences between them. Post-treatment, trichoscopic features of disease activity significantly decreased in all groups. Compared to control biopsies, both anagen follicles and decorin expression were significantly decreased in all pretreatment specimens. After treatment, all groups showed significantly increased anagen follicles and decorin expression compared to the baseline. Accordingly, FCL is an effective treatment for AA alone or combined with TA, PRP, or vitamin D3 solution. In AA, Decorin expression was downregulated, while enhanced expression following successful treatment occurred. This suggests the role of decorin in AA pathogenesis. However, further research is still recommended to clarify the exact role of decorin in AA pathogenesis and to investigate the therapeutic benefits of decorin-based therapy.

 
Research Authors
Azza Mahfouz Abdel Meguid, Alaa Ghazally, Asmaa M. Ahmed & Radwa M. Bakr
Research Date
Research Department
Research Journal
Archives of Dermatological Research
Research Publisher
Springer Berlin Heidelberg
Research Year
2023

Intralesional Candida albicans antigen versus intralesional zinc sulfate in treatment of cutaneous warts

Research Abstract

Immunotherapy represents a promising therapeutic option for treatment of warts. Different concentrations of Candida antigen (1/100 and 1/1000) and zinc sulfate 2% were not previously compared regarding their efficacy in treatment of cutaneous warts. The present study compared the safety and efficacy of intralesional candida antigen versus intralesional 2% zinc sulfate for treatment of cutaneous warts. This prospective controlled clinical trial included one hundred and five patients presented with common, plantar, and plane warts. Patients were divided randomly into three groups, each group included 35 patients. Group 1 were treated with intralesional candida antigen (Ag) 1/100, Group 2 were treated with intralesional candida Ag 1/1000, and Group 3 were treated with intralesional zinc sulfate 2%. This study found that target warts of group 1 displayed higher rate of complete clearance compared to group 2 and group 3 (94.3%, 77.1, 74.2%), respectively. The present study concluded that intralesional immunotherapy with Candida antigen was more effective than Intralesional 2% zinc sulfate in treatment of cutaneous warts and less painfulClinical trial registration number is (Clinical Trials.gov Identifier: NCT03158168).

Research Authors
Eman M Kamal Youssef, Maha AA Eissa, Radwa M Bakr
Research Date
Research Department
Research Journal
Archives of Dermatological Research
Research Pages
pages 1305–1314
Research Publisher
Springer Berlin Heidelberg
Research Vol
Volume 315
Research Year
2023
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